Synthesis of Thiazoline Complexes of Cu(ii), Ni(ii) and Co(ii) Transition Metals

Authors

  • Dinkar Malik Department of Chemistry, M. S. College, Saharanpur U.P. 1800/1, Mission Compound, Saharanpur, U.P.

DOI:

https://doi.org/10.53555/nnas.v3i1.669

Keywords:

Thiazoline Complexes, Electronic Studies, Fungicidal Activity, Heterocyclic Compounds

Abstract

The synthesis and characterization (elemental analysis, IR, electronic and magnetic susceptibility studies) of the transition metal complexes of Ni(II), Co(II) and Cu(II) with 2 - amino -4- (p- methoxy phenyl) thiazoline is described and complexes are obtained in 75-78% yield from the treatment of metal salts with ligand 2-amino- 4-(p-methoxy phenyl) thiazoline in 1:2 molar ratio in ethanolic medium. From the analytical and spectral data the stoichiometry of these complexes have been found to be of the type ML2X2 (where M = Cu (II), Co (II) and Ni (II)}.Evidences indicate that Ni(II), Cu(II) and Co(II) complexes exhibit octahedral and square planar geometry. The fungicidal activities of ligands and metal complexes were screened by growth method against various fungi i.e. Dreschlere setramera, Fusarium oxysporum, Macrophomera phaseoli at different concentrations. It is found that the activity decreases with decrease of concentration and the metal complexes are less toxic than the parent ligand.

References

Ashwini Khamamkar and Venkateshwar Pallapothula Rao. Synthesis, Spectral Characterization and Biological activity of Schiff’s base derived metal complexes. J. Ind. Council Chem, Vol 29(1&2), 2012, pp. 71-76

P.S. Mane, S.G. Shirodkar, B.R. Arbad and T.K. Chondhekar. Ind.. J. Chem, Sec A; Inorganic, Bio-inorganic, Physical & Analytical Chemistry, Vol. 40A(6), 2001, pp. 648.

Dinkar MaliK, Punam Yadav, Sandeep Kumar and Vijai Malik. Studies on Structural and biological aspects of transition metal complexes of the ligand 2-amino-4-(p-hydroxy phenyl) thiazole. Discovery Pharmacy, Vol 5(15), 2013, pp. 15-17.

S. Chandra and J. Sangeetika,. EPR and electronic spectral studies on copper(II) complexes of some N-O donor ligands, J. Indian Chem. Soc., Vol 81, 2004, pp. 203.

S.G.Shriodkar, P.S. Mane and T.K. Chondhekar. Synthesis and fungitoxic studies of Mn(II), Co(II), Ni(II) and Cu(II) with some heterocyclic Schiff base ligands, Indian J. Chem, Vol 40A, 2001, pp. 1114-1117.

S. Belaid, A. Landreau, O. Benali-Baitich, M.A. Khan and G. Bouet , Synthesis, characterisation and antifungal activity of a series of cobalt(II) and nickel(II) complexes with ligands derived from reduced N, N'-ophenylenebis (salicylideneimine), Trans. Met. Chem., Vol33, 2008, pp. 511.

A.K. Mapari and K.V. Mangaonkar. Synthesis, Characterization and Antimicrobial Activity of Mixed Ligand Complexes of N-(2-ethoxy-1-naphthylidene)-2,6-diisopropylaniline and N-(2-ethoxybenzylidene)-2,3-dimethylaniline with Co(II), Ni(II), Cu(II) and Zn(II) ions. International Journal of ChemTech Research.,Vol 3(2), 2011, pp. 636-641.

M. Ravanasiddappa, T. Sureshg, K. Syed, S.C. Radhavendray, C. Basavaraja and S.D. Angadi, Transition Metal Complexes of1, 4(2'-Ethoxyphenyl-1-yl) di-iminoazine: Synthesis, Characterization and Antimicrobial Studies, E-J. Chem.,Vol 5(2), 2008, pp. 395-403.

W. Manch and W. Fernelius Conard, The Structure and Spectra of Nickel(II) and Copper(II) Complexes, Journal of Chemical Education.,Vol 38 (4), 1961,pp. 192-201.

B. Naik and K. Desai, Novel approach for the rapid and efficient synthesis of heterocyclic Schiff bases and azetidinones under microwave irradiation, Indian journal of chemistry., Vol (45B), 2006, pp. 267-271.

S.K. Bharti, G. Nath, R. Tilak and S.K. Singh. Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring. Eur J Med Chem., Vol 45, 2010, pp. 651-660.

A.I. Vogal. Quantitative Organic Analysis., 1958.

A.I. Vogal. A Text Book of Quantitative Inorganic Analysis. 3rd ed. (English Language Book Society and Longman)., 1961.

R.M. Dodson and L.C. King. The reaction of ketones with halogens and thiourea J. Am. Chem. Soc.,Vol 67, 1945, pp. 2242.

N. Adibpour, A. Khalaj and S. Rajabalian. Synthesis and antibacterial activity of isothiazolyloxazolidinones and analogous 3(2H)-isothiazolones. Eur J Med Chem., Vol 45, 2010, pp. 19-24.

G. Aridoss, S. Amirthaganesan, M.S. Kim, J.T. Kim and Y.T. Jeong. Synthesis, spectral and biological evaluation of some new thiazolidinones and thiazoles based on t-3-alkyl-r-2, c-6-diarylpiperidin- 4-ones. Eur J Med Chem., Vol 44, 2009, pp. 4199-4210.

A. Arshad, H. Osman, M.C. Bagiey, C.K. Lan, S. Mohamad, A. Safirah and M. Zahariluddin Synthesis and antimicrobial properties of some new thiazolyl coumarin derivatives. Eur J Med Chem. 2022, pp., 1-7.

B.S. Dawane, S.G. Konda, G.G. Mandawad and B.M. Shaikh. Poly(ethylene glycol) (PEG-400) as an alternative reaction solvent for the synthesis of some new 1-(4- (4-chlorophenyl)-2-thiazolyl)-3-aryl-5-(2-butyl-4-chloro-1H-imidazol-5yl)-2-pyrazolines and their in vitro

antimicrobial evaluation. Eur J Med Chem., Vol 45, 2010, pp. 387-392.

R.S. Giri, H.M. Thaker, T. Giordano, J. Williams, D. Rogers, V. Sudersanam and K.K. Vasu. Design, Synthesis and characterization of novel 2-(2,4- disubstituted-thiazole-5-yl)-3-aryl-3Hquinazoline- 4-one derivatives as inhibitors of NF-IB and AP-1 mediated transcription activation and as potential anti-inflammatory agents. Eur J Med Chem., Vol 44, 2009, pp. 2184-2189.

A.M. Khalil, M.A. Berghot and M.A. Gouda. Synthesis and antibacterial activity of some new thiazole and thiophene derivatives. Eur J Med Chem., Vol 44, 2009, pp. 4434-4440.

V. Reddy, N. Patil and S.D. Angadi, Synthesis, Characterization and Antimicrobial Activity of Cu(II), Co(II) and Ni(II) Complexes with O, N, and S Donor Ligands, E-J. Chem.,Vol 5(3), 2008, pp. 577-583.

A. Earnshaw, Introductio to Magnetochemistry. Academic Press. New York., 1968.

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Published

2016-01-31

How to Cite

Malik, D. (2016). Synthesis of Thiazoline Complexes of Cu(ii), Ni(ii) and Co(ii) Transition Metals. Journal of Advance Research in Applied Science (ISSN 2208-2352), 3(1), 07-11. https://doi.org/10.53555/nnas.v3i1.669